Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, Ontario M5S 3G9, Canada.
Curr Opin Biotechnol. 2012 Oct;23(5):810-9. doi: 10.1016/j.copbio.2012.03.003. Epub 2012 Mar 21.
Human pluripotent stem cell (hPSC) differentiation aims to mimic development using growth factors or small molecules in a time-dependent and dose-dependent manner. However, the cell types produced using this approach are predominantly fetal-like in phenotype and function, limiting their use in regenerative medicine. This is particularly true in current efforts to produce pancreatic beta cells, wherein robust pancreatic progenitor maturation can only be accomplished upon transplantation into mice. Recent studies have suggested that hPSC-derived cells are capable of self-organizing in vitro, revealing a new paradigm for creating mature cells and tissues. Tissue engineering strategies that provide subtle and dynamic signals to developmentally naïve cells may be applied to mimic in vitro the self-organization aspects of pancreatic development.
人多能干细胞(hPSC)分化旨在通过生长因子或小分子在时间和剂量依赖的方式模拟发育。然而,使用这种方法产生的细胞类型在表型和功能上主要是胎儿样的,限制了它们在再生医学中的应用。在目前生产胰腺β细胞的努力中,这一点尤其如此,其中只有在移植到小鼠中时才能实现强大的胰腺祖细胞成熟。最近的研究表明,hPSC 衍生的细胞能够在体外自我组织,为创造成熟细胞和组织提供了新的范例。组织工程策略可以提供微妙和动态的信号给发育幼稚的细胞,从而在体外模拟胰腺发育的自我组织方面。